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  • Polymer and Materials Science  (7)
  • Wiley-Blackwell  (7)
  • 1
    Electronic Resource
    Electronic Resource
    Antiplasticization. III. Characteristics and properties of antiplasticizable polymersPaper presented at the 152nd National Meeting of the American Chemical Society, New York, September 1966.Prod. No. 1451 (1967)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 227-244 
    Details
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Antiplasticization is applicable to polymers which contain rigid, polar groups and stiff chains, such as many bisphenol polycarbonates and polyesters, 2,2,4,4-tetramethyl-1,3-cyclobutanediol polycarbonates and polyesters, cellulose triacetate, and a commercial poly(sulfone ether). The stiffness, hardness, and tensile strength of these polymers are increased by antiplasticizers, and the elongation, impact strength, and heat-distortion temperature are decreased. The stiffness of antiplasticized polymers can be further increased by crystallization. A clear, hard, stiff, tough, self-extinguishing molding plastic with good electrical properties and improved resistance to stress cracking is obtained by antiplasticizing bisphenol A polycarbonate with 20% Aroclor 5460.
    Additional Material: 9 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1967.070110206
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  • 2
    Electronic Resource
    Electronic Resource
    Chlorination of polyestersPaper presented at the 154th National Meeting of the American Chemical Society, Chicago, Illinois, September 10-15, 1967. (1968)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 1713-1733 
    Details
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: By photochemical chlorination chlorine was substituted on the gem-dimethyl groups of the polyterephthalate and polycarbonate of 2,2,4,4-tetramethyl-1,3-cyclobutanediol, the polyterephthalate of 2,2-dimethyl-1,3-propanediol, and the polycarbonate of 4,4′-isopropylidenediphenol (bisphenol A). The factors affecting polyester degradation, the efficiency of chlorination, and the degree of chlorination were investigated, and the effects of chlorine content on the solubility, flammability, density, hydrolytic stability, thermal stability, tensile properties, electrical properties, and heat-distortion temperatures of cast films were determined. The chlorinated polyesters of particular interest, because of their properties, are the polycarbonates of 2,2,4,4-tetramethyl-1,3-cyclobutanediol and bisphenol A.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1968.070120719
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  • 3
    Electronic Resource
    Electronic Resource
    Antiplasticization. II. Characteristics of antiplasticizersPaper presented at the 152nd National Meeting of the American Chemical Society, New York, September 1966.Prod. No. 1450 (1967)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 211-226 
    Details
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: By the incorporation of certain types of additives in bisphenol A polycarbonate, the modulus and tensile strength of the films are increased and the elongation is decreased. This effect is called antiplasticization, because the opposite results are obtained on plasticization - decreased modulus and tensile strength and increased elongation. A study of these additives indicated that antiplasticizers are compounds which are comptiable with the polymer and which (1) contain polar atoms such as halogen, nitrogen, oxygen, or sulfur, (2) contain at least two nonbridged rings, (3) have a glass transition temperature greater than -50°C., and (4) have one dimension less than about 5.5 A. in at least 65% of the length of the molecules.
    Additional Material: 8 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1967.070110205
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  • 4
    Electronic Resource
    Electronic Resource
    Properties of polyformals of alicyclic diolsPresented at the 142nd Meeting of the American Chemical Society, Atlantic City, New Jersey, September 9-14, 1962. (1963)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 1975-1981 
    Details
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The properties of the polyformals of several alicyclic diols were determined. Particularly unusual were the properties of the polyformal of 2,2,4,4-tetramethyl-1,3-cyclobutanediol. The polymer of the 1 : 1 cis/trans diol mixture had a reversible transition in crystalline phase at about 177°C. and a crystalline melting point of 262°C. The polymer was soluble in chloroform and in hot toluene. It was resistant to hydrolysis, particularly alkaline hydrolysis. Physical properties were determined on molded specimens obtained by injection-molding, on films obtained by casting and pressing, and on fibers obtained by melt-spinning.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1963.070070602
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  • 5
    Electronic Resource
    Electronic Resource
    Elastomers based on polycyclic bisphenol polycarbonatesPresented in part at the Polycarbonate Symposium, Southeastern Regional Meeting of the American Chemical Society, October 15-17, 1964, Charleston, West Virginia. (1965)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 3451-3463 
    Details
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Polycarbonate elastomers were prepared by the addition of phosgene to a pyridine solution of poly(tetramethylene ether) glycol and bisphenols containing norbornanetype groups. These elastomers do not contain the classical “tie-down” points - crosslinks, hydrogen bonding, or crystallinity - which, heretofore, have been considered necessary for good elastomer properties. This work introduces a new concept in elastomer chemistry: bulky, three-dimensional groups are effective tie-down points. Most of the elastomers were prepared with 4,4'-(2-norbornylidene)bis(2,6-dichlorophenol). For comparison, several elastomers with bisphenol-A were also prepared. A statistically designed experiment was carried out to determine the effect of composition variables on the properties of these elastomers. The properties were determined on films cast from methylene chloride and, in many cases, on wet-spun fibers. These elastomers have elongations of 400-600% and instantaneous elastic recoveries up to 100%.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1965.070091022
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  • 6
    Electronic Resource
    Electronic Resource
    Polyester hot-melt adhesives. I. Factors affecting adhesion to epoxy resin coatingsPresented at the 158th National Meeting of the American Chemical Society, New York, N. Y., September 1969. (1970)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 685-698 
    Details
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The peel strength and tensile shear strength of polyester hot-melt adhesives on metals coated with epoxy resins are affected by four characteristics of the polyester: (1) inherent viscosity, (2) glass transition temperature (Tg), (3) degree of crystallinity, and (4) melting point. The inherent viscosity affects the strength, toughness, and crystallinity of the adhesive. The Tg and degree of crystallinity affect the low-temperature adhesive properties; the peel strength is relatively low when the Tg is appreciably above the use temperature. The Tg, degree of crystallinity, and melting point affect the high-temperature adhesive properties. A hot-melt adhesive with high peel and tensile shear strengths from 0° to 120°C is the polyester of 1,4-butanediol and trans-1,4-cyclohexanedicarboxylic acid.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1970.070140313
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  • 7
    Electronic Resource
    Electronic Resource
    Interpolymerization of acrylonitrile and vinylidene chloride in tert-butyl alcohol (1960)
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 47 (1960), S. 397-402 
    Details
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: True interpolymers of acrylonitrile and vinylidene chloride were prepared with the use of tert-butyl alcohol or a mixture of tert-butyl alcohol and water as the polymerization solvent. Analysis of the polymers showed that the ratio of the two monomers in the copolymers was very close to the initial monomer ratio. The polymers were tested for homogeneity by their solubility in acetone or acetonitrile.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1960.1204714935
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